CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Antifungal prophylaxis and pre-emptive therapy: When and how?
Antifungal prophylaxis and pre-emptive therapy: When and how?
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
危重或免疫功能低下患者群体的不断增长,导致由曲霉属、念珠菌属和耶氏肺孢子菌等真菌引起的危及生命的侵袭性感染持续增加。针对这一情况,已为高风险患者群体制定并实施了预防性和抢先抗真菌治疗策略。风险降低所带来的获益需要与长期暴露于抗真菌药物可能造成的潜在危害进行仔细权衡。这包括不良反应、耐药性的产生以及医疗系统的成本。在这篇综述中,我们总结了证据并讨论了在急性白血病、造血干细胞移植、CAR-T 细胞治疗和实体器官移植等恶性肿瘤背景下抗真菌预防和抢先治疗的优点与缺点。
我们还讨论了腹部手术后和病毒性肺炎患者以及遗传性免疫缺陷个体的预防策略。血液学研究已取得显著进展,关于抗真菌预防和抢先治疗的强烈推荐得到了随机对照试验数据的支持,而其他关键领域仍缺乏高质量证据。在这些领域,确定性数据的缺乏转化为基于现有数据解读、当地专业知识和流行病学的各中心特定策略。新型免疫调节抗癌药物的开发、高端重症监护治疗以及具有新作用机制、不良反应和给药途径的新型抗真菌药物的研发,将对未来的预防性和抢先治疗策略产生影响。
The growing pool of critically ill or immunocompromised patients leads to a constant increase of life-threatening invasive infections by fungi such as Aspergillus spp. , Candida spp. and Pneumocystis jirovecii. In response to this, prophylactic and pre-emptive antifungal treatment strategies have been developed and implemented for high-risk patient populations. The benefit by risk reduction needs to be carefully weighed against potential harm caused by prolonged exposure against antifungal agents.
This includes adverse effects and development of resistance as well as costs for the healthcare system. In this review, we summarise evidence and discuss advantages and downsides of antifungal prophylaxis and pre-emptive treatment in the setting of malignancies such as acute leukaemia, haematopoietic stem cell transplantation, CAR-T cell therapy, and solid organ transplant.
We also address preventive strategies in patients after abdominal surgery and with viral pneumonia as well as individuals with inherited immunodeficiencies. Notable progress has been made in haematology research, where strong recommendations regarding antifungal prophylaxis and pre-emptive treatment are backed by data from randomized controlled trials, whereas other critical areas still lack high-quality evidence.
In these areas, paucity of definitive data translates into centre-specific strategies that are based on interpretation of available data, local expertise, and epidemiology. The development of novel immunomodulating anticancer drugs, high-end intensive care treatment and the development of new antifungals with new modes of action, adverse effects and routes of administration will have implications on future prophylactic and pre-emptive approaches.
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